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The Saccharomyces cerevisiae DNA Recombination and Repair Functions of the RAD52 Epistasis Group Inhibit Ty1 Transposition
Alison J. Rattraya, Brenda K. Shafera, and David J. Garfinkelaa Gene Regulation and Chromosome Biology Laboratory, ABL-Basic Research Program, NCI-FCRDC, Frederick, Maryland 21702
Corresponding author: Alison J. Rattray, Gene Regulation and Chromosome Biology Laboratory, ABL-Basic Research Program, NCI-FCRDC, P.O. Box B, Bldg. 539, Rm. 151, Frederick, MD 21702., rattray{at}mail.ncifcrf.gov (E-mail)
Communicating editor: L. S. SYMINGTON
) elements. Here we examine the role of the cellular homologous recombination functions on Ty1 transposition. We find that transposition is elevated in cells mutated for genes in the RAD52 recombinational repair pathway, such as RAD50, RAD51, RAD52, RAD54, or RAD57, or in the DNA ligase I gene CDC9, but is not elevated in cells mutated in the DNA repair functions encoded by the RAD1, RAD2, or MSH2 genes. The increase in Ty1 transposition observed when genes in the RAD52 recombinational pathway are mutated is not associated with a significant increase in Ty1 RNA or proteins. However, unincorporated Ty1 cDNA levels are markedly elevated. These results suggest that members of the RAD52 recombinational repair pathway inhibit Ty1 post-translationally by influencing the fate of Ty1 cDNA.
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